Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.

Abnormalities, Multiple Autoradiography Catalase/blood Child, Preschool Chromosome Aberrations Chromosome Disorders Chromosomes, Human, 13-15 Dermatoglyphics Female Foot Hand Haptoglobins/blood Humans Intellectual Disability Karyotyping

Haptoglobins Catalase